Maestro 711-299MCQRecalls & reported problems
Ortho Organizers, Inc. · Maestro® .018 Kit U/L 5x5 MC HKS · Class 1
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Apr 2, 2019Terminated
Orthodontic Bracket is mislabeled
Z-2478-2020 · Root cause: Process control · FDA record ↗
Other BRACKET, METAL, ORTHODONTIC devices
- Maestro 711-298QOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 recall0 reports
- Maestro 711-206-10Ortho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 recall0 reports
- Carriere 424-925CNOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC2 reports
- Carriere 424-917RNOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
- Carriere® SLX 3D™ 777-UR1-10Ortho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
- Carriere 425-425ROrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
- Carriere 424-916CNOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
- Carriere 424-922LNOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.